<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE168nnn/GSE168638/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species> Schizosaccharomyces pombe</species><species>Saccharomyces cerevisiae</species><gds_type>Expression profiling by array</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE168638</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Expression data from budding yeast sec12-4 and sec12-4 ino2Δino4Δ mutant cells</name><description>Sec12 is a guanine nucleotide exchange factor (GEF) required for the initiation of COPII vesicle formation in ER to Golgi transport. The sec12-4 mutant cells show temperature sensitivity in growth and a defect in ER-to-Golgi protein transport. Ino2/Ino4 are components of the heteromeric basic helix-loop-helix transcription activator that binds inositol/choline-responsive elements (ICREs) and are required for derepression of phospholipid biosynthetic genes in response to inositol depletion. We used microarrays to compare the global gene expression profiles between sec12-4 and sec12-4 ino2Δino4Δmutant cells.</description><dates><publication>2026/04/01</publication></dates><accession>GSE168638</accession><cross_references><GSM>GSM5151936</GSM><GSM>GSM5151939</GSM><GSM>GSM5151937</GSM><GSM>GSM5151938</GSM><GSM>GSM5151940</GSM><GSM>GSM5151941</GSM><GPL>2529</GPL><GSE>168638</GSE><taxon> Schizosaccharomyces pombe</taxon><taxon>Saccharomyces cerevisiae</taxon></cross_references></HashMap>